Canonical Allele Identifier: CA371892601

Gene: EXT1

Linked Data

• MyVariant Identifiers: chr8:g.118847761A>T (hg19) ; chr8:g.117835522A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117835522A>T , CM000670.2:g.117835522A>T	GRCh38
NC_000008.10:g.118847761A>T , CM000670.1:g.118847761A>T	GRCh37
NC_000008.9:g.118916942A>T	NCBI36
NG_007455.2:g.281298T>A , LRG_493:g.281298T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684189.1:n.553T>A
ENST00000378204.7:c.1086T>A MANE Select	ENSP00000367446.3:p.Asn362Lys
ENST00000436216.2:c.454T>A
ENST00000378204.6:c.1086T>A	ENSP00000367446.2:p.Asn362Lys
ENST00000436216.1:c.454T>A
ENST00000437196.1:c.103T>A	ENSP00000407299.1:p.Trp35Arg
NM_000127.2:c.1086T>A , LRG_493t1:c.1086T>A	NP_000118.2:p.Asn362Lys
NM_000127.3:c.1086T>A MANE Select	NP_000118.2:p.Asn362Lys